A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268909



Internal ID20478127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58613766..58613831hg38UCSC Ensembl
chr17:56691127..56691192hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747573
Supporting Variants
Samples
Known GenesTEX14
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268909
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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